• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

剪接体U5小核仁RNA末端环1中修饰核苷酸的系统发育保守性。

Phylogenetic conservation of modified nucleotides in the terminal loop 1 of the spliceosomal U5 snRNA.

作者信息

Szkukalek A, Myslinski E, Mougin A, Luhrmann R, Branlant C

机构信息

Laboratoire d'Enzymologie et de Génie Génétique, URA-CNRS 457, Université de Nancy I, Faculté des Sciences, Vandoeuvre-les-Nancy, France.

出版信息

Biochimie. 1995;77(1-2):16-21. doi: 10.1016/0300-9084(96)88099-0.

DOI:10.1016/0300-9084(96)88099-0
PMID:7599272
Abstract

In order to study the phylogenetic conservation of modified nucleotides in the spliceosomal U5 snRNA, we determined the nucleotide sequences of the U5 snRNAs from the slime mold Physarum polycephalum (EMBL data bank accession numbers: X74440 and X74441) and we identified the pseudouridine and 2'-O-methylated residues. From a comparison of all the U5 snRNAs studied at the level of nucleotide modifications, we concluded that the modified nucleotides in U5 snRNA can be divided into three classes according to their degree of conservation: i) the modified nucleotides of the 5' terminal cap structure that display some variations from one species to the other; ii) the modified nucleotides located in the helical part of the stem/loop structure I that vary greatly in number, position and identity from one species to the other; and iii) the modified nucleotides of the terminal loop 1, that are almost identical in all the species studied. Taking into account the recent discovery of a crucial role played by this terminal loop of U5 snRNA in 5' and 3' splice site definition, we postulate that the numerous modified nucleotides it contains, five out of a total of 11, play an important role in spliceosome assembly and function. Their possible role is discussed.

摘要

为了研究剪接体U5小核仁RNA(snRNA)中修饰核苷酸的系统发育保守性,我们测定了黏菌多头绒泡菌U5 snRNA的核苷酸序列(EMBL数据库登录号:X74440和X74441),并鉴定了假尿苷和2'-O-甲基化残基。通过在核苷酸修饰水平上对所有研究的U5 snRNA进行比较,我们得出结论,U5 snRNA中的修饰核苷酸可根据其保守程度分为三类:i)5'末端帽结构的修饰核苷酸,在不同物种间存在一些差异;ii)位于茎环结构I螺旋部分的修饰核苷酸,其数量、位置和种类在不同物种间差异很大;iii)末端环1的修饰核苷酸,在所有研究的物种中几乎相同。考虑到最近发现U5 snRNA的这个末端环在5'和3'剪接位点定义中起关键作用,我们推测它所含的众多修饰核苷酸(总共11个中有5个)在剪接体组装和功能中起重要作用。文中讨论了它们可能的作用。

相似文献

1
Phylogenetic conservation of modified nucleotides in the terminal loop 1 of the spliceosomal U5 snRNA.剪接体U5小核仁RNA末端环1中修饰核苷酸的系统发育保守性。
Biochimie. 1995;77(1-2):16-21. doi: 10.1016/0300-9084(96)88099-0.
2
Pseudouridine modification in Caenorhabditis elegans spliceosomal snRNAs: unique modifications are found in regions involved in snRNA-snRNA interactions.秀丽隐杆线虫剪接体snRNA中的假尿苷修饰:在参与snRNA - snRNA相互作用的区域发现独特修饰。
BMC Mol Biol. 2005 Oct 19;6:20. doi: 10.1186/1471-2199-6-20.
3
A limited number of pseudouridine residues in the human atac spliceosomal UsnRNAs as compared to human major spliceosomal UsnRNAs.与人类主要剪接体UsnRNAs相比,人类atac剪接体UsnRNAs中的假尿苷残基数量有限。
RNA. 1999 Nov;5(11):1495-503. doi: 10.1017/s1355838299991537.
4
Patterns of conservation of spliceosomal intron structures and spliceosome divergence in representatives of the diplomonad and parabasalid lineages.二联体纲和原生动物亚界代表生物的剪接体内含子结构和剪接体进化的保守模式。
BMC Evol Biol. 2019 Aug 2;19(1):162. doi: 10.1186/s12862-019-1488-y.
5
snRNA interactions at 5' and 3' splice sites monitored by photoactivated crosslinking in yeast spliceosomes.通过酵母剪接体中的光活化交联监测5'和3'剪接位点处的小核RNA相互作用。
RNA. 1995 Nov;1(9):968-80.
6
Spliceosomal snRNA modifications and their function.剪接体小核 RNA 修饰及其功能。
RNA Biol. 2010 Mar-Apr;7(2):192-204. doi: 10.4161/rna.7.2.11207. Epub 2010 Mar 14.
7
Localization of modified nucleotides in Schizosaccharomyces pombe spliceosomal small nuclear RNAs: modified nucleotides are clustered in functionally important regions.粟酒裂殖酵母剪接体小核RNA中修饰核苷酸的定位:修饰核苷酸聚集在功能重要区域。
RNA. 1996 Sep;2(9):909-18.
8
Modified nucleotides at the 5' end of human U2 snRNA are required for spliceosomal E-complex formation.人U2小核RNA 5'端的修饰核苷酸是剪接体E复合物形成所必需的。
RNA. 2004 Dec;10(12):1925-33. doi: 10.1261/rna.7186504. Epub 2004 Nov 3.
9
Conservation of functional features of U6atac and U12 snRNAs between vertebrates and higher plants.脊椎动物和高等植物之间U6atac和U12小核RNA功能特征的保守性。
RNA. 1999 Apr;5(4):525-38. doi: 10.1017/s1355838299982213.
10
The 3.8 Å structure of the U4/U6.U5 tri-snRNP: Insights into spliceosome assembly and catalysis.U4/U6.U5 三 snRNP 的 3.8Å 结构:剪接体组装和催化的深入了解。
Science. 2016 Jan 29;351(6272):466-75. doi: 10.1126/science.aad6466. Epub 2016 Jan 7.

引用本文的文献

1
Spliceosomal snRNA Epitranscriptomics.剪接体小核核糖核酸表观转录组学
Front Genet. 2021 Mar 2;12:652129. doi: 10.3389/fgene.2021.652129. eCollection 2021.
2
Orchestrated positioning of post-transcriptional modifications at the branch point recognition region of U2 snRNA.U2小核RNA分支点识别区域转录后修饰的精心定位。
RNA. 2018 Jan;24(1):30-42. doi: 10.1261/rna.063842.117. Epub 2017 Sep 29.
3
Small Cajal body-specific RNAs of Drosophila function in the absence of Cajal bodies.果蝇的小型 Cajal 体特异性 RNA 在没有 Cajal 体的情况下发挥作用。
Mol Biol Cell. 2009 Dec;20(24):5250-9. doi: 10.1091/mbc.e09-09-0777.
4
RNomics in Drosophila melanogaster: identification of 66 candidates for novel non-messenger RNAs.黑腹果蝇中的RNA组学:66种新型非信使RNA候选物的鉴定。
Nucleic Acids Res. 2003 May 15;31(10):2495-507. doi: 10.1093/nar/gkg361.
5
Mutations in U5 snRNA loop 1 influence the splicing of different genes in vivo.U5小核仁RNA环1中的突变在体内影响不同基因的剪接。
Nucleic Acids Res. 2002 Dec 15;30(24):5476-84. doi: 10.1093/nar/gkf692.
6
Proximity of the invariant loop of U5 snRNA to the second intron residue during pre-mRNA splicing.前体mRNA剪接过程中U5小核仁RNA的恒定环与第二个内含子残基的接近度。
EMBO J. 2001 Jul 2;20(13):3577-86. doi: 10.1093/emboj/20.13.3577.
7
A small nucleolar guide RNA functions both in 2'-O-ribose methylation and pseudouridylation of the U5 spliceosomal RNA.一种小核仁引导RNA在U5剪接体RNA的2'-O-核糖甲基化和假尿苷化过程中均发挥作用。
EMBO J. 2001 Feb 1;20(3):541-51. doi: 10.1093/emboj/20.3.541.
8
A limited number of pseudouridine residues in the human atac spliceosomal UsnRNAs as compared to human major spliceosomal UsnRNAs.与人类主要剪接体UsnRNAs相比,人类atac剪接体UsnRNAs中的假尿苷残基数量有限。
RNA. 1999 Nov;5(11):1495-503. doi: 10.1017/s1355838299991537.
9
Conserved loop I of U5 small nuclear RNA is dispensable for both catalytic steps of pre-mRNA splicing in HeLa nuclear extracts.U5小核RNA的保守环I对于HeLa细胞核提取物中前体mRNA剪接的两个催化步骤都是可有可无的。
Mol Cell Biol. 1999 Apr;19(4):2782-90. doi: 10.1128/MCB.19.4.2782.
10
Pseudouridine mapping in the Saccharomyces cerevisiae spliceosomal U small nuclear RNAs (snRNAs) reveals that pseudouridine synthase pus1p exhibits a dual substrate specificity for U2 snRNA and tRNA.在酿酒酵母剪接体U小核RNA(snRNA)中进行假尿苷定位揭示,假尿苷合酶pus1p对U2 snRNA和tRNA表现出双重底物特异性。
Mol Cell Biol. 1999 Mar;19(3):2142-54. doi: 10.1128/MCB.19.3.2142.